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Merck
CN

W245615

丙酸乙酯

greener alternative

natural, ≥97%, FCC, FG

别名:

Ethyl propanoate, Propanoic acid ethyl ester, n-Ethyl propanoate

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关于此项目

线性分子式:
CH3CH2COOC2H5
化学文摘社编号:
105-37-3
分子量:
102.13
FEMA Number:
2456
Council of Europe no.:
402c
UNSPSC Code:
12164502
PubChem Substance ID:
24901102
Flavis number:
9.121
EC Number:
203-291-4
NACRES:
NA.21
MDL number:
MFCD00009308
Beilstein/REAXYS Number:
506287
Organoleptic:
grape; fruity; ethereal; rum; sweet; wine-like
Grade:
FG
Halal
Kosher
natural
Agency:
meets purity specifications of JECFA
Food allergen:
no known allergens

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产品名称

丙酸乙酯, natural, ≥97%, FCC, FG

SMILES string

CCOC(=O)CC

InChI

1S/C5H10O2/c1-3-5(6)7-4-2/h3-4H2,1-2H3

InChI key

FKRCODPIKNYEAC-UHFFFAOYSA-N

grade

FG
Halal
Kosher
natural

agency

meets purity specifications of JECFA

reg. compliance

EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 117

vapor density

3.52 (vs air)

vapor pressure

40 mmHg ( 27.2 °C)

assay

≥97%

autoignition temp.

887 °F

expl. lim.

11 %

greener alternative product characteristics

Less Hazardous Chemical Syntheses
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

refractive index

n20/D 1.384 (lit.)

bp

99 °C (lit.)

mp

−73 °C (lit.)

density

0.888 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

greener alternative category

, Aligned

organoleptic

grape; fruity; ethereal; rum; sweet; wine-like

Quality Level

300
400

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相关类别

General description

We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product is a Biobased products, showing key improvements in Green Chemistry Principles “Less Hazardous Chemical Syntheses” and “Use of Renewable Feedstock”.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

3 - Flammable liquids

wgk

WGK 1

flash_point_f

53.6 °F - closed cup

flash_point_c

12 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SHBQ4337
SHBP2887
SHBN5831
SHBN3432
SHBL8796

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O Esch et al.
Hepatology (Baltimore, Md.), 18(2), 373-379 (1993-08-01)
We performed experiments in anesthetized piglets with two cholesterol gallstone solvents, methyl tert-butyl ether and ethyl propionate, to determine whether blood levels of either solvent would increase during gallbladder instillation of these solvents under conditions simulating gallstone dissolution. The solvent
C Y Chen et al.
Digestive diseases and sciences, 40(2), 419-426 (1995-02-01)
We evaluated the toxic effects of four currently used chemolytic solvents--dimethyl sulfoxide (DMSO, 99%), ethyl propionate (EP, 99%), tetrasodium ethyl-dimethyl tetraacetate (4Na-EDTA, 2%, pH 11), and methyl tert-butyl ether (MTBE, purity = 99.5%) in an animal model. Each solvent was
Vibeke F Andersen et al.
The journal of physical chemistry. A, 116(21), 5164-5179 (2012-04-25)
Ethyl propionate is a model for fatty acid ethyl esters used as first-generation biodiesel. The atmospheric chemistry of ethyl propionate was investigated at 980 mbar total pressure. Relative rate measurements in 980 mbar N(2) at 293 ± 0.5 K were
A F Hofmann et al.
Digestive diseases and sciences, 42(6), 1274-1282 (1997-06-01)
Topical dissolution of cholesterol gallbladder stones using methyl tert-butyl ether (MTBE) is useful in symptomatic patients judged too ill for surgery. Previous studies showed that ethyl propionate (EP), a C5 ester, dissolves cholesterol gallstones rapidly in vitro, but differs from
Sun-Liang Cui et al.
The Journal of organic chemistry, 72(20), 7779-7782 (2007-09-11)
A novel synthesis of Hantzsch-type N-substituted 1,4-dihydropyridines from salicaldehydes, ethyl propiolate, and amines has been developed. Salicaldehydes were treated with ethyl propiolate in the presence of N-methylmorpholine to give ethyl 3-(2-formylphenoxy)propenoates. Three equivalents of ethyl 3-(2-formylphenoxy)propenoates reacted with 1 equiv
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